Avian 4-type adenovirus vector, construction method and attenuated live vaccine and application of avian 4-type adenovirus vector
A technology of live attenuated vaccines and adenoviruses, applied in the direction of viruses/bacteriophages, viruses, vaccines, etc., can solve problems that have not yet been reported on live attenuated vaccines
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Embodiment 1
[0053] Embodiment 1, construction of intermediate plasmid pAMS9002
[0054] The schematic diagram of the construction of the intermediate plasmid pAMS9002 is as follows: figure 1 As shown, the specific construction steps include:
[0055] (1) Digest the FAdV-4 genome with MauBI and SpeI (see Genbank accession number: MG547384 for the nucleotide sequence of the FAdV-4 genome), and use the kit after electrophoresis (Zymoclean Large FragmentDNA Recovery Kit, Cat.D4045, Zymo Research company) recovered an 8953bp fragment, which contains the open reading frames of ORF16, ORF17, GAM-1, ORF29, ORF28, ORF43, ORF42, ORF20, ORF20A and ORF22 on the right side of the FAdV-4 genome;
[0056] (2) Under standard polymerase chain reaction (PCR) conditions, using the plasmid vector pMD18-T as a template, use the primers shown in Table 1 below (the following primers are synthesized by BGI) to amplify the ORI of 2326bp - AMP fragment, containing the origin of replication (ORI) of the pBR322 pl...
Embodiment 2
[0062] Embodiment 2, the construction of intermediate plasmid pAMS-XGAM1
[0063] The schematic diagram of the construction of the intermediate plasmid pAMS-XGAM1 is as follows: figure 2 As shown, the specific construction steps include:
[0064] (1) Use BsiW I / Eag I to double digest the pAMS9002 plasmid, and recover a 10014bp fragment by electrophoresis; (2) Use the pAMS9002 plasmid as a template, and perform PCR amplification with the primers in the following Table 2 (the following primers are synthesized by Huada Gene) , the 705bp XGAM-1 fragment (SEQ ID NO: 3) was obtained and recovered by electrophoresis, and about 30bp at both ends of the fragment were identical to the sequence at both ends of the 10014bp fragment recovered above;
[0065] Table 2
[0066]
[0067] Note: Due to the use of DNA assembly technology, the 2010XGAM1f primer may not contain the BsiW I restriction site, and the 2010XGAM1r primer happens to contain the Eag I restriction site.
[0068] (3) ...
Embodiment 3
[0071] Embodiment 3, the construction of recombinant adenovirus plasmid pkFAV4-CXGA
[0072] The schematic diagram of the construction of the recombinant adenovirus plasmid pkFAV4-CXGA is as follows: image 3 As shown, the specific construction steps include:
[0073] (1) Use Pac I to digest the pAMS-XGAM1 plasmid, and recover a large fragment of 8385bp after electrophoresis; the large fragment of 8385bp does not contain an ORI-AMP fragment.
[0074] (2) Digest the pKFAV4-CX19A plasmid with MauB I / Spe I.
[0075] It should be noted that the pKFAV4-CX19A plasmid is a plasmid that has been disclosed in the prior art, and the construction method is described in YAN Bingyu, ZOU xiaohui et al. User-Friendly Reverse Genetics System for Modification of the Right End of Fowl Adenovirus 4 Genome. Viruses 2020, 12(3), 301.
[0076] Specifically, the pKFAV4-CX19A plasmid comprises the origin of replication of the pBR322 plasmid, the kanamycin resistance gene and the FAdV-4 genome (see...
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